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nsv5559677

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 117 SVs from 20 studies. See in: genome view    
Submitted genomic203,405,629-203,405,636Question Mark
Overlapping variant regions from other studies: 117 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):204,270,352-204,270,359Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5559677Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2203,405,629203,405,636
nsv5559677RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2204,270,352204,270,359

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16922930sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16922930Submitted genomicNC_000002.12:g.203
405629_203405636in
s388
GRCh38 (hg38)NC_000002.12Chr2203,405,629203,405,636
nssv16922930RemappedPerfectNC_000002.11:g.204
270352_204270359in
s388
GRCh37.p13First PassNC_000002.11Chr2204,270,352204,270,359

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16922930<0.00126402
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